bio-tcr-bcr-analysis-repertoire-visualization — independently scanned and version-tracked by SaferSkills.
SaferSkills independently audited bio-tcr-bcr-analysis-repertoire-visualization (Agent Skill) and scored it 100/100 (green). The audit ran 55 deterministic rules across Security, Supply Chain, Maintenance, Transparency, and Community; it found 0 high-severity and 0 lower-severity findings. The full rule-by-rule trace and per-finding evidence are below. Free, methodology-open.
Findings & checks · 0 flagged
Every scanned point with the score it earned and what moved between them.
First recorded scan — no prior version to compare against.
The primary manifest — the file an agent reads to learn what this artifact does.
Reference examples tested with: MiXCR 4.6+, VDJtools 1.2.1+, ggplot2 3.5+, matplotlib 3.8+, pandas 2.2+, scanpy 1.10+, seaborn 0.13+
Before using code patterns, verify installed versions match. If versions differ:
pip show <package> then help(module.function) to check signaturespackageVersion('<pkg>') then ?function_name to verify parameters<tool> --version then <tool> --help to confirm flagsIf code throws ImportError, AttributeError, or TypeError, introspect the installed package and adapt the example to match the actual API rather than retrying.
"Visualize my immune repertoire data" → Create publication-quality figures for TCR/BCR repertoires including circos plots, V(D)J gene usage heatmaps, diversity plots, and clonal tracking across samples.
vdjtools PlotFancyVJUsage for circos-style V-J plotsmatplotlib/seaborn for custom repertoire visualizations# Generate V-J usage circos plot
vdjtools PlotFancyVJUsage \
-m metadata.txt \
output_dir/
# Generates PDF circos plots showing V-J pairing frequenciesimport pandas as pd
import matplotlib.pyplot as plt
from pycircos import Gcircle
def plot_vj_circos(clone_df):
'''Create circos plot of V-J usage'''
# Count V-J pairs
vj_counts = clone_df.groupby(['v_gene', 'j_gene']).size().reset_index(name='count')
# Create circos
circle = Gcircle()
# Add arcs for each V and J gene
v_genes = vj_counts['v_gene'].unique()
j_genes = vj_counts['j_gene'].unique()
# Add sectors and links
# ... (complex setup)
circle.save('vj_circos.pdf')library(circlize)
plot_vj_circos <- function(clone_df) {
# Prepare adjacency matrix
vj_matrix <- table(clone_df$v_gene, clone_df$j_gene)
# Create circos plot
chordDiagram(
vj_matrix,
transparency = 0.5,
annotationTrack = c("grid", "name")
)
}import pandas as pd
import matplotlib.pyplot as plt
def plot_clone_tracking(clones_by_time, top_n=10):
'''Track top clones across timepoints'''
# Get top clones by total frequency
total_freq = clones_by_time.groupby('cdr3_aa')['frequency'].sum()
top_clones = total_freq.nlargest(top_n).index
fig, ax = plt.subplots(figsize=(10, 6))
for clone in top_clones:
clone_data = clones_by_time[clones_by_time['cdr3_aa'] == clone]
ax.plot(clone_data['timepoint'], clone_data['frequency'],
marker='o', label=clone[:20])
ax.set_xlabel('Timepoint')
ax.set_ylabel('Clone Frequency')
ax.legend(bbox_to_anchor=(1.05, 1), loc='upper left')
plt.tight_layout()
plt.savefig('clone_tracking.pdf')import matplotlib.pyplot as plt
import seaborn as sns
def plot_diversity_comparison(diversity_df, metric='shannon'):
'''Compare diversity between groups'''
fig, ax = plt.subplots(figsize=(8, 6))
sns.boxplot(
data=diversity_df,
x='condition',
y=metric,
ax=ax
)
sns.stripplot(
data=diversity_df,
x='condition',
y=metric,
color='black',
alpha=0.5,
ax=ax
)
ax.set_ylabel(f'{metric.capitalize()} Diversity')
plt.savefig('diversity_comparison.pdf')def plot_overlap_heatmap(overlap_matrix):
'''Plot pairwise repertoire overlap'''
import seaborn as sns
fig, ax = plt.subplots(figsize=(10, 8))
sns.heatmap(
overlap_matrix,
annot=True,
fmt='.2f',
cmap='YlOrRd',
ax=ax
)
ax.set_title('Repertoire Overlap (Jaccard Index)')
plt.tight_layout()
plt.savefig('overlap_heatmap.pdf')def plot_spectratype(clone_df, group_col=None):
'''Plot CDR3 length distribution'''
fig, ax = plt.subplots(figsize=(10, 6))
clone_df['cdr3_length'] = clone_df['cdr3_nt'].str.len()
if group_col:
for group, data in clone_df.groupby(group_col):
ax.hist(data['cdr3_length'], bins=range(20, 80, 3),
alpha=0.5, label=group, density=True)
ax.legend()
else:
ax.hist(clone_df['cdr3_length'], bins=range(20, 80, 3))
ax.set_xlabel('CDR3 Length (nt)')
ax.set_ylabel('Density')
ax.set_title('CDR3 Length Distribution (Spectratype)')
plt.savefig('spectratype.pdf')import networkx as nx
def plot_clone_network(clone_df, similarity_threshold=0.8):
'''Create network of similar clonotypes'''
from Levenshtein import ratio
G = nx.Graph()
clones = clone_df['cdr3_aa'].unique()
# Add nodes
for clone in clones:
freq = clone_df[clone_df['cdr3_aa'] == clone]['frequency'].sum()
G.add_node(clone, size=freq)
# Add edges for similar clones
for i, c1 in enumerate(clones):
for c2 in clones[i+1:]:
sim = ratio(c1, c2)
if sim >= similarity_threshold:
G.add_edge(c1, c2, weight=sim)
# Draw network
fig, ax = plt.subplots(figsize=(12, 12))
pos = nx.spring_layout(G)
sizes = [G.nodes[n]['size'] * 1000 for n in G.nodes()]
nx.draw(G, pos, node_size=sizes, with_labels=False, ax=ax)
plt.savefig('clone_network.pdf')~30 seconds. Free. No account. Every finding cites a rule and a line of evidence.